Hanna Shalev

Mutation of TRPM6 causes familial hypomagnesemia with secondary hypocalcemia

Roxanne Y. Walder, Daniel Landau, Peter Meyer et al. · Nature Genetics · 2002 · 561 citations

Mendelian Disorder, Genetic Disorder, Genetics +5

CATSPER2, a human autosomal nonsyndromic male infertility gene

Nili Avidan, Hannah Tamary, Orly Dgany et al. · European Journal of Human Genetics · 2003 · 206 citations · Full text

Infertility, Andrology, Fertility +5

Congenital Dyserythropoietic Anemia Type I Is Caused by Mutations in Codanin-1

Orly Dgany, Nili Avidan, J. Delaunay et al. · The American Journal of Human Genetics · 2002 · 166 citations · Full text

Mendelian Disorder, Genetic Disorder, Genetics +8

Elevated growth differentiation factor 15 expression in patients with congenital dyserythropoietic anemia type I

Hannah Tamary, Hanna Shalev, Galit Perez‐Avraham et al. · Blood · 2008 · 139 citations · Full text

Mutated <i>nup62</i> causes autosomal recessive infantile bilateral striatal necrosis

Lina Basel‐Vanagaite, Liora Muncher, Rachel Straussberg et al. · Annals of Neurology · 2006 · 133 citations